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Preoperative Precautions/Intraoperative Suprises

Preoperative Precautions
Preoperative calculations of the IOL require painstaking care, and if not performed correctly can result in postoperative refractive error disasters. The range ofpostoperative refractive error that patients will be happy with today is narrow. They expect to see well uncorrected immediately after cataract surgery; to meet this expectation, surgeons must determine the correct IOL power measurement.

To achieve that accuracy, you must avoid several potential pitfalls in the preoperative workup: Perhaps most vulnerable to surgeon error are axial length measurement and keratometry, essential factors in IOL power calculations. (For more information, see "Nine Ways to Improve Your IOL Calculations," April 1999.)

Complicating the issue even further is that our cataract patient population now includes individuals who have undergone refractive surgery. A significant, and rapidly growing, number of patients seen every day in U.S. cataract practices have had radial keratotomy, astigmatic keratotomy or a laser refractive procedure. The resultant comeal changes can be challenging when determining IOL power.

In general, the most efficient way to accurately calculate the intraocular lens power in these eyes is to identify the keratometry prior to the refractive procedure, as well as the amount of refractive error corrected at that time. As a general principle, the current axial length measured is included in the surgeon's favorite IOL calculation formula. The original average keratometry is used after the amount of refractive error previously corrected is subtracted. For example, if the patient's original keratometry reading before the refractive procedure was 45 D, and that patient had a PRK to correct -6 D, the effective keratometry reading for the IOL calculation formula would be 45 - 6, or SOD (average keratometry).

Accurate A-scans are also critical, and achieving the correct measurement can be challenging, especially for newly trained technicians, in highly myopic patients who may have staphylomas that can cause variable measurements. Very high myopic or hyperopic axial lengths challenge even the most sophisticated IOL calculation formulas. Most of these measurement problems can be avoided by using the surgeon's favorite algorithm routinely; experience with one formula can maximize the accuracy of the results.

Intraoperative Surprises
A variety of intraoperative problems can challenge cataract surgery. Though most are not serious, their management does significantly affect the outcome of the procedure. Important factors that need to be assessed at the end of cataract extraction and before IOL implantation are:

  1. Stability and structure of the cataract wound.
  2. The condition of the anterior capsulotomy.
  3. The amount of the zonular support.
  4. Posterior capsular integrity.

If there is no problem with the wound, the anterior capsule has no tears, there is good zonular support and the posterior capsule is intact, then a foldable intraocular lens can be implanted and unfolded within the capsular bag. If a problem exists in one of these areas, you must reconsider the decision to implant an IOL in the bag.

One rare but significant problem is an artifact, flaw or damage in the intraocular lens. Every surgeon should carefully evaluate the structure and integrity of the intraocular lens prior to its implantation, even in the "20th case of the day."

Take foldable lOLs, for example. Most of these lenses are folded in the operating room before implantation. The folding process itself can bend or break the haptics and scratch, break or cause permanent striae in the optic. Noting damage before beginning to implant the lens or before completing implantation in the capsular bag allows the surgeon to replace the damaged IOL.

If the damage is seen after the lens is implanted, then the surgeon faces explanting the now unfolded intraocular lens from the anterior chamber or the capsular bag and replacing it with another lens. If you encounter this scenario, consider these options: Either enlarge the incision (if it is scleral), or work through a second scleral incision, or bisect the lens into two pieces for easier explantation.

An abrupt release of the haptic and/or optic from the IOL injector or other folding instrument is another possible problem with foldable lOLs. This uncontrolled release can cause such severe trauma to the posterior capsule that IOL implantation is compromised. In these cases, it is prudent to avoid vitreous prolapse by limiting intraocular manipulations until you have devised an appropriate surgical plan. If vitreous prolapse is present, I suggest completing a thorough anterior vitrectomy, and then deciding whether the unfolded IOL can be placed in the capsular bag or if it can be stabilized in the sulcus. If you decide that the foldable IOL, now unfolded in the eye, will not be stable within the residual capsular bag or the sulcus (usually the case with lenses of smaller total diameter), remove the IOL and replace it with a larger total diameter lens that can be sulcus-fixated. If there is not sufficient capsular support, an anterior chamber intraocular lens may be inserted. Also consider a posterior chamber, scleral-fixated intraocular lens.

If zonular dehiscence occurs, IOL implantation can be quite challenging. One option is to attempt sulcus fixation. Another is the use of a capsular expansion ring. Several companies market these rings, which usually are made of PMMA and are very easy to implant within the capsular bag. Their total diameter varies between 11 and 13 mm. They expand once placed within the capsule and provide better bag stability for posterior chamber intraocular lenses, especially in cases with poor zonular support or compromised capsular bags. I have successfully used these rings several weeks postoperatively to help correct IOL subluxation due to partial zonular dehiscence.

 
 
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